Label: NOSK EX SLEEP- menthol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 14, 2016

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active Ingredient: Menthol 2.0%

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Alcohol, Glycerin, Dipropylene glycol, Gossypium Herbaceum(cotton) seed extract, Magnolia Kubus Bark extract, Lilium tigrinum extract, Paeonia albiflora root extract, Carbomer, Disodium EDTA, Triethanolamine

  • PURPOSE

    Purpose: Skin Refresher

  • Caution

    Caution: - For the external use only . - Do not apply to eyes ,wounds , broken skin and deep puncture wounds - For 7 years and older only. - When using this product do not get into eyes, Stop use and ask a doctor if rash occurs - Keep out of reach of children - It is recommend to stop applying and to talk to dermatologist immediately if you are suffering such conditions a rash, swell up and itchness - Do not leave it on high, low temperature or exposed on sunlight

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS & USAGE

    Indications and usage: 1. Apply to back of neckand, cervical vertebrae and shoulder , make you awake and refreshment. 2. Shake well up and down before use Push a little the ball on apply , liquid easily out.

  • DOSAGE & ADMINISTRATION

    Dosage and administration: Take an adequate amount of this product.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    NOSK EX SLEEP 
    menthol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70767-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) Menthol0.2 g  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Alcohol (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70767-010-026 in 1 CARTON05/01/2016
    1NDC:70767-010-0110 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/01/2016
    Labeler - DreamAir Co., (689846965)
    Registrant - DreamAir Co., (689846965)
    Establishment
    NameAddressID/FEIBusiness Operations
    DreamAir Co.,689846965manufacture(70767-010)